FIBER OPTIC ILLUMINATOR 8065751577

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-10 for FIBER OPTIC ILLUMINATOR 8065751577 manufactured by Alcon Research, Ltd. - Houston.

Event Text Entries

[92748654] A product sample has been received by the manufacturer and it is awaiting evaluation. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[92748655] A surgeon reported an infusion cannula was inserted into a broken trocar cannula and an irrigation failure occurred which caused an ocular hypotony during a procedure. The procedure was completed without product replacement. There was no harm to the patient. No additional information is expected.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644019-2017-00791
MDR Report Key7017995
Date Received2017-11-10
Date of Report2018-02-01
Date of Event2017-10-12
Date Mfgr Received2018-01-08
Device Manufacturer Date2017-04-19
Date Added to Maude2017-11-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. NADIA BAILEY
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8176152230
Manufacturer G1ALCON RESEARCH, LTD. - HOUSTON
Manufacturer Street9965 BUFFALO SPEEDWAY
Manufacturer CityHOUSTON TX 77054
Manufacturer CountryUS
Manufacturer Postal Code77054
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NameFIBER OPTIC ILLUMINATOR
Generic NameLIGHT, SURGICAL, FIBEROPTIC
Product CodeFST
Date Received2017-11-10
Returned To Mfg2017-11-08
Model NumberNA
Catalog Number8065751577
Lot Number2005823H
Device Expiration Date2019-03-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerALCON RESEARCH, LTD. - HOUSTON
Manufacturer Address9965 BUFFALO SPEEDWAY HOUSTON TX 77054 US 77054


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-11-10

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